Neudle.com: gene analysis

Differential
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aciduria

acoustic neurinoma

acoustic neurinoma, bilateral

acquired immunodeficiency syndrome

adrenoleukodystrophy

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

Alzheimer's disease, diagnosis of

Alzheimer's disease, early onset

Alzheimer's disease, familial

amniocentesis

amyloid

amyloid angiopathy, cerebral

amyloid angiopathy, hereditary cystatin C

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, familial

apraxia of eye movements

arteriopathy

ataxia

ataxia telangiectasia

attention deficit disorder with hyperactivity

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

Babinski sign

basal ganglia

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

benign familial neonatal convulsions

brachial neuritis

brachial plexus neuropathy

brachial plexus neuropathy, familial

brain biopsy

brainstem, lesion of

brainstem, neoplasms of

bulbar palsy, progressive

cafe au lait spots

calcification, intracranial

calcitonin gene-related peptide receptor blocker

cane

carcinoembryonic antigen

carcinoma

carcinoma of pancreas

CAT scan

CAT scan, abnormal

cataracts

caudate nucleus, atrophy

cavernous hemangioma

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebellum, neoplasms of

cerebral atherosclerosis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral infarction

cerebral infarction, subcortical

cerebral ischemia

cerebral palsy

cerebro hepato renal syndrome

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, young adult

choreoathetosis, paroxysmal

chromosomal abnormality

clubfoot as related to neurologic disease

Cockayne's syndrome

cognition

coma

compression neuropathy

compression neuropathy, recurrent

corpus callosum, lesion of

cost effectiveness

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cryptococcal meningitis

cyst, neoplastic cerebellum

cytomegalovirus infection

degenerative diseases of CNS

dementia

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, transmissible

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental retardation

diabetes mellitus

diagnostic criteria

differential diagnosis

disability rating scale, neurological

DNA probes

dopa responsive dystonia

drooling

drug induced neurologic disorders

dysarthria

dysmorphic

dystonia

dystonia musculorum deformens

electronystagmography

electroretinograph

encephalitis

encephalitis, autoimmune

encephalitis, focal

encephalitis, Rasmussen's

encephalitis, viral

enzyme, muscle disease

epidemiology of neurology

ethics in neurology

eye movement, disorders of

Fabry's disease

face, elongated

facial appearance, abnormal

familial

fasciculation

fatal familial insomnia

fragile-X syndrome

Friedreich's ataxia

fundus, abnormality of

gadolinium

gait disorder

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

GFAP gene

globus pallidus

globus pallidus, lesion of, bilateral

GLUT1 deficiency syndrome

gonadotropin-releasing hormone

growth retardation

gynecomastia

hair analysis

Hallervorden Spatz disease

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

Huntington's chorea, genetic counselling

Huntington's chorea, presymptomatic detection of

Huntington's disease, children

hyperactivity

hyperekplexia

hyperhidrosis

hyperkalemic periodic paralysis

immunoperoxidase staining

immunosuppression

in situ hybridization

inborn errors of metabolism

inclusion bodies, intracytopasmic

insomnia

intellectual deficit

intellectual deterioration

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, young adult

iron, brain

Jakob-Creutzfeldt disease

joint hypermobility

Kallmann's syndrome

Kearns-Sayre syndrome

KRIT1 gene

Kugelberg-Welander syndrome

lacunar infarction

Laurence-Moon-Bardet-Biedl syndrome

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

malignant hyperpyrexia

manic-depressive

medulla oblongata

medulla oblongata, atrophy

medulla oblongata, lesion of

memory, impairment of

meningitis

meningitis, recurrent

meningitis, relapse

mental retardation

mental retardation, familial

metachromatic leukodystrophy

Mexican

Mexico

microcephaly

microhemorrhage, intracerebral

migraine

migraine, children

migraine, pathogenesis

migraine, prophylaxis

migraine, treatment of

monoclonal antibodies

mononeuropathy

mononeuropathy, recurrent

mortality

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, eye of tiger sign

MRI, gradient-echo

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

mucopolysaccharidoses

mucopolysacchariduria

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

multiple system atrophy

muscular dystrophy, Becker

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, Duchenne, presymptomatic detection

muscular dystrophy, female occurrence of

muscular dystrophy, limb-girdle

myelin basic protein gene

myoclonus

myopathy

myopathy, mitochondrial

neonatal screening, genetic neurologic disorders

neoplasm, metastatic to CNS

neoplasm, posterior fossa

neoplasm, primary intracranial

neoplasm, primary of CNS

neurocutaneous disease

neurodegeneration with brain iron accumulation

neurofibromatosis 2, presymptomatic

neurologic disease

neurologic disease, diagnoses of

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuropathology

neuropathology, brain

neuropathy

neuropathy, amyloid

neuropathy, hereditary peripheral

neuropathy, peripheral

neurotomy

next-generation sequencing

night blindness

nonsteroidal anti-inflammatory drug

Notch3 gene

ocular motility, disorders of

oculopharyngeal muscular dystrophy

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

Parkinsonism syndrome

paroxysmal dystonic choreoathetosis

paroxysmal neurologic deficits

pathology

patient information and support

periodic paralysis

peroxisomal disease

pheochromocytoma

pigmentary retinopathy

polycystic kidneys

polymerase chain reaction

polyneuropathy, familial

posterior fossa, lesion of

practice guidelines

prenatal diagnosis by amniocentesis

presenilin-1 gene

presenilin-2 gene

prevention of neurologic disorders

prion disease

progeria

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive spinal muscular atrophy

proximal myotonic myopathy

pseudobulbar palsy

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

radiation hypersensitivity

seizure, intractable, treatment of

seizure, neonatal

sensorineural hearing loss

serotonin agonist

simian crease

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

small vessel disease

small vessel disease, cerebral

Southern immunoblot test

spastic ataxia

spasticity

spinal cord

spinal cord, lesion of

spinal cord, neoplasm

spinal muscular atrophy

spine, metastasis to

spinocerebellar ataxia

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spondylosis

spongy degeneration of brain

startle reaction

striatal encephalitis

stuporous

subarachnoid hemorrhage

synkinesis

tapetoretinal degeneration

telangiectases

testicular enlargement

thalamus, lesion of

tinnitus

tomaculous neuropathy

trauma

treatment of neurologic disorder

trigeminovascular system

trinucleotide repeats

triptans

Usher's syndrome

ventricular garlands

vibratory sensation, abnormal

Von Hippel Lindau, carrier

Von Hippel Lindau, screening protocol for

walking, difficulty with

Werdnig-Hoffman disease

Western immunoblot test

wheelchair

white matter disease

white matter disease, subcortical

workup

X-linked bulbospinal neuronopathy

x-linked mental retardation

X-linked neuropathy

Showing articles 1750 to 1800 of 1870 << Previous Next >>

Hereditary Myoclonus & Progressive Distal Muscular Atrophy
Ann Neurol 6:227-231, Jankovic,J.,et al, 1979

Agenesis of the Corpus Callosum:A Study of the Frequency of Associated Malformations
Ann Neurol 6:349-354, Parrish,M.L.,et al, 1979

Quadriceps Myopathy in Two Brothers
Rhode Island Med J 62:125, Finelli,P.F., 1979

Familial Lumbar Spinal Stenosis with Acute Disc Herniation, Case Reports of Four Brothers
J Neurosurg 51:234-236, Varughese,G.,et al, 1979

Familial Inverted Choreoathetosis
Neurol 29:1627-1631, Fisher,M.,et al, 1979

Abnormal Iris Vasculature in Myotonic Dystrophy
Arch Neurol 35:224, Stern,L.Z.,et al, 1978

Nemaline (Rod) Myopathy:The Need for Histochemical Evaluation of Affected Families
Ann Neurol 4:37, Bender,A.N.,et al, 1978

Leigh's Disease in an Adult with Evidence of"Inhibitor Factor"in Family Members
Ann Neurol 3:519, Whetsell,W.O.,et al, 1978

Familial Hypopituitarism with Large Sella Turcica
NEJM 298:698, Parks,J.S.,et al, 1978

Familial Occurrence of Meralgia Paresthetica
Arch Neurol 35:182, Massey,E.W., 1978

Meningiomas in Five Members of a Family Over Two Generations, in One Member Simultaneously with Acoustic Neurinomas
Neurol 28:567, Delleman,J.W.,et al, 1978

Normal Pressure Hydrocephalus, Recog & Relation to Neuro Abnormalities in Cockayne's Sydrome
Arch Neurol 35:337, Brumback,R.A.,et al, 1978

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

The Cherry-red Spot-Myoclonus Syndrome
Ann Neurol 3:234, Rapin,I.,et al, 1978

Familial Cavernous Angiomas
Arch Neurol 35:746-749, Bicknell,J.M.,et al, 1978

Monozygotic Twins With Presumed Metachromatic Leukodystrophy
Arch Neurol 35:689-691, Hashimoto,T.,et al, 1978

Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978

Familial Incidence of Ruptured Intracranial Aneurysms
Arch Neurol 35:675-677, Acosta-Rua,G.J., 1978

Ataxia Telangiectasia
Arch Neurol 35:553-554, Teplitz,R.L., 1978

Tics & Tourette's:A Continuum of Symptoms
Ann Neurol 4:145-148, Golden,G.S., 1978

Precautions in Familial Transmissible Dementia
Arch Neurol 35:697-698, Cook,R.,et al, 1978

Obstructive Sleep Apnea in Family Members
NEJM 299:969-973, Strohl,K.P.,et al, 1978

Neurological Manifestations of Hereditary Hemorrhagic Telangiectasia (Rendu-Osler-Weber Disease)
Ann Neurol 4:130-144, Roman,G.,et al, 1978

Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
Neurol 28:1135-1140, Dobkin,B.H.,et al, 1978

Peripheral Neuropathy in Myotonic Dystrophy
Arch Neurol 35:741-745, Olson,N.D.,et al, 1978

Systemic Membrane Defect in the Proximal Muscular Dystrophies
NEJM 299:841-846, Pickard,N.A.,et al, 1978

Mirror Movements after Childhood Hemiparesis
Neurol 28:1152-1158, Woods,B.T.,et al, 1978

The Lissencephaly, (Agyria) Syndrome in Siblings
Arch Neurol 35:608-611, Garcia,C.A.,et al, 1978

Familial Chorea & Myoclonus Epilepsy
Neurol 28:913-919, Takahata,N.,et al, 1978

Clinical pathological conference
Von Hippel-Lindau disease, Case Record 1-1978, NEJM 298:95978., , 1978

NERVLINE, A Neuroscience Information Retrieval System
Neurol 28:380, Finelli,P.F., 1978

Hereditary Paroxysmal Ataxia:Response to Acetazolamide
Neurol 28:1259-1264, Griggs,R.C.,et al, 1978

Clinical Syndromes of Myasthenia in Infancy & Childhood
Arch Neurol 35:97, Fenichel,G.M., 1978

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Familial Vascular Malformation or Chance Occurrence
Neurol 28:98, Barre,R.G.,et al, 1978

Supratentorial Leptomeningeal Hemangioblastoma
Neurol 28:727, Lee,K.R.,et al, 1978

Blue Rubber Bleb Nevus Syndrome with CNS Involvement & Thrombosis of a Vein of Galen Malformation
Ann Neurol 3:464, Waybright,E.A.,et al, 1978

Extreme Insulin Resistance in Ataxia Telangiectasia
NEJM 298:1164, Bar,R.S.,et al, 1978

Familial Degeneration of the Basal Ganglia with Acanthocytosis:a Clinical Neuropathological, & Neurochemical Study
Ann Neurol 3:253, Bird,T.D.,et al, 1978

Diagnosis of Treatable Wilson's Disease
NEJM 298:1347, Cartwright,G.E., 1978

Dominant Spinopontine Atrophy
Arch Neurol 35:156, Pogacar,S.,et al, 1978

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Malignant Hyperthermia & Central Core Disease in a Child with Congenital Dislocating Hips
Arch Neurol 35:189, Eng,G.D.,et al, 1978

Pseudoxanthoma Elasticum:A Review of Neurological Complications
Ann Neurol 4:18, Iqbal,A.,et al, 1978

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Muscle Fiber-Type Disproportion
Arch Neurol 35:823-826, Eisler,T.,et al, 1978

Autosomal Dominant Neurological Disorders
Ann Neurol 4:548-552, Brady,R.O.,et al, 1978

Adrenomyeloneuropathy:A Probable Variant of Adrenoleukodystrophy
Neurol 27:1107-1113, Griffin,J.W.,et al, 1977

Neuroectodermal Tumors in the Cerebellum in Two Sisters
JNNP 40:886, Thomas,M.,et al, 1977

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

Showing articles 1750 to 1800 of 1870 << Previous Next >>